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UT Health San AntonioNew
Overview
The research assistant will coordinate and participate in clinical research activities including participant recruitment, consenting, and cognitive assessments. They will also perform administrative duties, data entry, and quality control reviews while working closely with investigators.
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Compensation
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UTHealth Houston
Coordinate day-to-day operations for clinical research studies, including participant recruitment, enrollment, and data management. Assist with regulatory submissions, budget preparation, and the creation of research papers and reports.
4 days ago
University of Virginia
The coordinator will recruit, screen, consent, and enroll participants in oncology clinical trials while building relationships with patients and collecting high-quality data at study visits. Key duties involve maintaining accurate documentation, processing lab specimens, tracking adverse events, and ensuring strict protocol and regulatory compliance.
$33 - $92 / HOUR
7 days ago
Vanderbilt University Medical Center
The Research Nurse Specialist 2 maintains the integrity and quality of clinical research trials, planning recruitment, managing enrollment, and ensuring protocol compliance under occasional guidance. Key duties include preparing research proposals, performing administrative tasks, utilizing nursing skills for procedures, and observing/reporting adverse events.
10 days ago
University of Miami
The Clinical Research Coordinator 2 assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. This role involves day-to-day operations of clinical research protocol implementation and study coordination duties from protocol initiation to study close-out.
11 days ago
Duke Careers
This role involves managing all aspects of clinical research operations within the Anesthesiology Clinical Research Unit, including preparing FDA regulatory submissions, managing investigational products, and ensuring protocol compliance across various settings.
$59,829 - $99,960 / YEAR
12 days ago
The specialist will support clinical research operations by managing participant documentation, data collection, and regulatory compliance for cancer studies. They will also collaborate with investigators to facilitate participant recruitment, study visits, and the preparation of research materials.
$21 - $31 / HOUR
13 days ago
ICON plc
The Clinical Research Nurse I will support the execution of clinical trials by assisting in planning, implementation, and coordination of research activities while conducting patient assessments and administering study treatments. This role involves collecting, recording, and maintaining accurate patient data in eCRFs and collaborating with multidisciplinary teams to ensure efficient study conduct and participant retention.
17 days ago
University of Massachusetts Medical School
The Clinical Research Coordinator manages human subject research protocols, including regulatory documentation, participant visits, and data collection. They ensure compliance with federal and institutional guidelines while supporting investigators with grant preparation and study reporting.
20 days ago
The Clinical Research Coordinator I is responsible for coordinating regulatory activities and managing data collection for research protocols. This includes obtaining consent from participants, scheduling study visits, and ensuring compliance with protocols.
22 days ago
UVA Health
The coordinator will recruit, screen, consent, and enroll participants in oncology clinical trials, building relationships with patients while coordinating study visits and collecting high-quality data. Key duties involve maintaining accurate documentation, processing lab specimens, tracking adverse events, and ensuring strict protocol and regulatory compliance.
23 days ago
The Clinical Research Coordinator II will coordinate regulatory activities and manage data collection for complex research protocols. They will also ensure compliance with study protocols and assist with participant interactions and documentation.
$48,000 - $55,000
The Clinical Research Support Specialist assists in the recruitment, screening, and enrollment of study participants while managing data collection and regulatory documentation. They also conduct community outreach, schedule research visits, and maintain consistent communication with participants to ensure study adherence.
24 days ago
NCIRE - The Northern California Institute for Research and Education, Inc.
Coordinate and manage clinical trials focusing on PTSD, TBI, and sleep disorders, combining research tasks with administrative operations. Responsibilities include collecting psychophysiological data, managing regulatory documents, and overseeing participant recruitment and scheduling.
$25 - $41 / HOUR
29 days ago
UTHealth (University of Texas Health Science Center at Houston)
Coordinate day-to-day operations for clinical research studies, including participant recruitment, consenting, and visit scheduling. Manage data collection, regulatory submissions, and the preparation of research reports and grant proposals.
1 month ago
Johns Hopkins University
The coordinator will administratively manage clinical protocol implementation and ensure the logistical execution of study activities. Key duties include participant recruitment, consenting, data collection, and coordinating submissions to the Institutional Review Board.
$17 - $30 / HOUR
Ann & Robert H. Lurie Children's Hospital of Chicago
The Research Coordinator II will manage research projects, including participant recruitment, data collection, and quality assurance. They will also coordinate with clinical partners and community organizations to ensure adherence to study protocols.
$49,920 - $81,619 / YEAR
The Clinical Research Coordinator will manage the daily operations of clinical trials, ensuring adherence to study protocols and safety regulations. They will serve as the primary liaison between the Principal Investigator, regulatory agencies, and study participants while handling recruitment, data collection, and documentation.
The Clinical Research Coordinator will manage the logistical implementation of clinical protocols and ensure adherence to study activities. They will also provide administrative support for regulatory issues, including IRB submissions and participant recruitment.
University of Rochester
The Human Subject Research Specialist II coordinates clinical trial activities, including participant enrollment, protocol implementation, and data management within the infectious disease division. They ensure compliance with regulatory standards, maintain research records, and assist with quality assurance audits.
$25 - $35 / HOUR
